Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PanAd3-RSV + MVA-RSV is an investigational viral-vectored vaccine candidate for respiratory syncytial virus (RSV) infection. The vaccine utilizes a heterologous prime-boost regimen consisting of two components: PanAd3-RSV, a replication-defective chimpanzee-derived adenovirus vector, and MVA-RSV, a modified vaccinia virus Ankara vector. Both vectors are engineered to express three RSV antigens: the fusion (F) protein (in a truncated soluble form, F0ΔTM), the nucleocapsid (N) protein, and the matrix (M2-1) protein. This combination is designed to induce a balanced immune response, including both neutralizing antibodies (humoral immunity) and robust T-cell responses (cellular immunity), without the Th2-biased cytokines associated with vaccine-enhanced respiratory disease. The vaccine has been evaluated in Phase 1 clinical trials for safety and immunogenicity in healthy younger and older adults.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on PanAd3-RSV + MVA-RSV.